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Clinical Trials/NCT04407728
NCT04407728
Unknown
Not Applicable

Early Detection of Severe Heart Disease in Fetuses at High Risk of Heart

University Hospital, Grenoble0 sites500 target enrollmentNovember 15, 2020
ConditionsHeart Diseases

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Heart Diseases
Sponsor
University Hospital, Grenoble
Enrollment
500
Primary Endpoint
early ultrasound screening
Last Updated
5 years ago

Overview

Brief Summary

The main objective of the work is to evaluate, in the French health care system, the performance of early ultrasound screening for severe heart disease between 11 and 14SA in high-risk populations.

Detailed Description

Numerous studies have shown a link between increased nuchal translucency and heart disease. Although high-risk fetal populations are identified between 11 and 13 SA on clinical and biological criteria and by screening ultrasound (Echo T1), cardiac morphology analysis is routinely performed only during 2nd trimester fetal morphology ultrasound between 18 and 22 SA (EchoMorpho-T2) inducing a difficult wait for the couple. The development of increasingly efficient ultrasound probes has made it possible to explore the foetal heart at an earlier stage. International learned societies recommend an early morphological examination with heart-centered slices before 14 weeks in high-risk situations. This practice is not systematic in France and no study has evaluated its feasibility and impact in a French care network.

Registry
clinicaltrials.gov
Start Date
November 15, 2020
End Date
November 2, 2022
Last Updated
5 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Sponsor
University Hospital, Grenoble
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Pregnant women whose fetus is at high risk for congenital heart disease:
  • Nuchal translucency measurement on T1 echo ≥3.5mm
  • Cardiac or extra-cardiac morphological abnormality suspected on the T1 screening echo
  • First degree family history for the fetus (patient, spouse, 1st children of the couple) of significant congenital cardiopathy (excluding AIC, muscular VIC or persistent CA).

Exclusion Criteria

  • Multiple Pregnancies
  • non-emancipated minors, persons unable to express their consent.
  • Lack of affiliation to a social security scheme.
  • Subject in a period of exclusion from another study,
  • Subject under administrative or judicial supervision
  • Subject cannot be contacted in case of emergency

Outcomes

Primary Outcomes

early ultrasound screening

Time Frame: 1 day

Calculation of the sensitivity and specificity of screening for severe heart disease using EchoMorpho-T1. Specificity will be privileged in order to avoid the anxiety-producing nature of false positives.

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